Literature DB >> 24372406

Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction.

J Foster1, S Kapoor, O Diaz-Horta, A Singh, C Abad, A Rastogi, R Moharana, O Tekeli, K Walz, M Tekin.   

Abstract

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Year:  2013        PMID： 24372406     DOI： 10.1111/cge.12321

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  4 in total

1.  IGSF3 mutation identified in patient with severe COPD alters cell function and motility.

Authors:  Kelly S Schweitzer; Natini Jinawath; Raluca Yonescu; Kevin Ni; Natalia Rush; Varodom Charoensawan; Irina Bronova; Evgeny Berdyshev; Sonia M Leach; Lucas A Gillenwater; Russel P Bowler; David B Pearse; Constance A Griffin; Irina Petrache
Journal:  JCI Insight       Date:  2020-07-23

2.  Preliminary report on screening IGSF3 gene mutation in families with congenital absence of lacrimal puncta and canaliculi.

Authors:  Fei Wang; Hai Tao; Cui Han; Fang Bai; Peng Wang; Xi-Bin Zhou; Li-Hua Wang; Chuan Liu
Journal:  Int J Ophthalmol       Date:  2020-09-18       Impact factor: 1.779

3.  Molecular Profiling of the Developing Lacrimal Gland Reveals Putative Role of Notch Signaling in Branching Morphogenesis.

Authors:  Galina Dvoriantchikova; Wensi Tao; Steve Pappas; Gabriel Gaidosh; David T Tse; Dmitry Ivanov; Daniel Pelaez
Journal:  Invest Ophthalmol Vis Sci       Date:  2017-02-01       Impact factor: 4.799

4.  Malformation of Tear Ducts Underlies the Epiphora and Precocious Eyelid Opening in Prickle 1 Mutant Mice: Genetic Implications for Tear Duct Genesis.

Authors:  Jiali Ru; Dianlei Guo; Jiaying Fan; Jiao Zhang; Rong Ju; Hong Ouyang; Lai Wei; Yizhi Liu; Chunqiao Liu
Journal:  Invest Ophthalmol Vis Sci       Date:  2020-11-02       Impact factor: 4.799
  4 in total

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